phentermine hydrochloride

Generic: phentermine hydrochloride

Labeler: pd-rx pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name phentermine hydrochloride
Generic Name phentermine hydrochloride
Labeler pd-rx pharmaceuticals, inc.
Dosage Form CAPSULE
Routes
ORAL
Active Ingredients

phentermine hydrochloride 30 mg/1

Manufacturer
PD-Rx Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 72789-287
Product ID 72789-287_3cf6a04a-fac4-c523-e063-6294a90a37ac
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA205019
DEA Schedule civ
Listing Expiration 2026-12-31
Marketing Start 2017-01-24

Pharmacologic Class

Classes
appetite suppression [pe] increased sympathetic activity [pe] sympathomimetic amine anorectic [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 72789287
Hyphenated Format 72789-287

Supplemental Identifiers

RxCUI
900038
UPC
0372789287300
UNII
0K2I505OTV

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name phentermine hydrochloride (source: ndc)
Generic Name phentermine hydrochloride (source: ndc)
Application Number ANDA205019 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 30 mg/1
source: ndc
Packaging
  • 14 CAPSULE in 1 BOTTLE, PLASTIC (72789-287-14)
  • 28 CAPSULE in 1 BOTTLE, PLASTIC (72789-287-28)
  • 30 CAPSULE in 1 BOTTLE, PLASTIC (72789-287-30)
source: ndc

Packages (3)

72789-287-14 14 CAPSULE in 1 BOTTLE, PLASTIC (72789-287-14) 72789-287-28 28 CAPSULE in 1 BOTTLE, PLASTIC (72789-287-28) 72789-287-30 30 CAPSULE in 1 BOTTLE, PLASTIC (72789-287-30)

Ingredients (1)

phentermine hydrochloride (30 mg/1)

Linked Drug Pages (1)

Phentermine Hydrochloride ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "3cf6a04a-fac4-c523-e063-6294a90a37ac", "openfda": {"upc": ["0372789287300"], "unii": ["0K2I505OTV"], "rxcui": ["900038"], "spl_set_id": ["e4508aa9-1e7a-4af7-829e-5fa353c92f5e"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "14 CAPSULE in 1 BOTTLE, PLASTIC (72789-287-14)", "package_ndc": "72789-287-14", "marketing_start_date": "20221115"}, {"sample": false, "description": "28 CAPSULE in 1 BOTTLE, PLASTIC (72789-287-28)", "package_ndc": "72789-287-28", "marketing_start_date": "20250507"}, {"sample": false, "description": "30 CAPSULE in 1 BOTTLE, PLASTIC (72789-287-30)", "package_ndc": "72789-287-30", "marketing_start_date": "20221115"}], "brand_name": "Phentermine Hydrochloride", "product_id": "72789-287_3cf6a04a-fac4-c523-e063-6294a90a37ac", "dosage_form": "CAPSULE", "pharm_class": ["Appetite Suppression [PE]", "Increased Sympathetic Activity [PE]", "Sympathomimetic Amine Anorectic [EPC]"], "product_ndc": "72789-287", "dea_schedule": "CIV", "generic_name": "phentermine hydrochloride", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Phentermine Hydrochloride", "active_ingredients": [{"name": "PHENTERMINE HYDROCHLORIDE", "strength": "30 mg/1"}], "application_number": "ANDA205019", "marketing_category": "ANDA", "marketing_start_date": "20170124", "listing_expiration_date": "20261231"}